A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17097344



Internal ID21406801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85395372..85395372hg38UCSC Ensembl
chr13:85969507..85969507hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5650912
Supporting Variants
SamplesHG00512
Known GenesLINC00351
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17097344
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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